Optimal Timing of Antiretroviral Therapy Initiation in Acquired Immunodeficiency Syndrome–Associated Toxoplasmic Encephalitis: A Prospective Observational Multicenter Study in China

Bibliographic Details
Title: Optimal Timing of Antiretroviral Therapy Initiation in Acquired Immunodeficiency Syndrome–Associated Toxoplasmic Encephalitis: A Prospective Observational Multicenter Study in China
Authors: Yao Li, Haidong Jiang, Yanming Zeng, Yanqiu Lu, Siyuan Chen, Yulin Zhang, Zhongsheng Jiang, Tongtong Yang, Shuiqing Liu, Yaokai Chen, Haijuan Wang
Source: ​​​​​​​​Infectious Diseases & Immunity, Vol 4, Iss 1, Pp 4-9 (2024)
Publisher Information: Wolters Kluwer Health - Lippincott Williams Wilkins, 2024.
Publication Year: 2024
Collection: LCC:Infectious and parasitic diseases
Subject Terms: Infectious and parasitic diseases, RC109-216
More Details: Abstract. Background. Toxoplasmic encephalitis (TE) is the most frequent cause of expansive brain lesions among patients with acquired immunodeficiency syndrome (AIDS). However, the optimal timing of antiretroviral therapy (ART) initiation in these patients remains controversial. This study aims to investigate the differences in outcomes of ART initiation at different times, in order to help clarify the treatment timing of AIDS-associated TE. Methods. This multicenter prospective observational study included 87 patients recruited from 11 research centers in China (from March 2019 to December 2022). Of the patients, 38 were assigned to the early ART group (initiating ART within 2 weeks after anti-Toxoplasma treatment initiation), and the remaining 49 patients received deferred ART (initiating ART at least 2 weeks after anti-Toxoplasma treatment initiation). The main outcomes included mortality and emergence of immune reconstitution inflammatory syndrome (IRIS). Human immunodeficiency virus (HIV)-1 viral load and CD4+ T-cell counts at weeks 24 and 48 were observed. Results. The number of deaths (1 vs. 5, P = 0.225) and incidence of IRIS (2.6% vs. 0, P = 0.437) were not significantly different between the early and deferred ART groups at week 48. Early ART initiation did not contribute significantly to HIV-1 viral load control (
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2096-9511
2693-8839
00000000
Relation: http://journals.lww.com/10.1097/ID9.0000000000000105; https://doaj.org/toc/2096-9511; https://doaj.org/toc/2693-8839
DOI: 10.1097/ID9.0000000000000105
Access URL: https://doaj.org/article/62f5d05fb38146f59f598577ca3a662d
Accession Number: edsdoj.62f5d05fb38146f59f598577ca3a662d
Database: Directory of Open Access Journals
More Details
ISSN:20969511
26938839
00000000
DOI:10.1097/ID9.0000000000000105
Published in:​​​​​​​​Infectious Diseases & Immunity
Language:English